A method to recover and harvest nutrients and volatile gases such as alcohols from a liquid stream using a fixed film bioreactor. The method includes a means of concentrating product gas stripped from a bioreactor.

Patent
   9464303
Priority
Dec 29 2010
Filed
Nov 20 2014
Issued
Oct 11 2016
Expiry
Dec 01 2031

TERM.DISCL.
Assg.orig
Entity
Small
40
20
EXPIRED
1. A process for recovering volatile and non-volatile products from a substrate-laden influent stream using microorganisms growing in a rotating bioreactor contactor, said bioreactor including a vessel, a shaft mounted for rotation within said vessel about a shaft axis, a plurality of axially spaced-apart, growth plates attached to the shaft, each of the plates having surfaces to which a fixed film of the microorganisms are attached, and means for rotating the shaft and plates about the axis, comprising the simultaneous steps of:
(a) operating the rotating bioreactor as an aerobic, facultative or anaerobic reactor;
(b) feeding the influent stream past the growth plates such that the growth plates are partially submerged within the stream, whereby, as they grow, the microorganisms convert the substrate to volatile products and accumulate biomass; and
(c) passing a stripping gas past the growth plates to harvest the volatile products as stripped gas.
12. A process for concentrating the chemical constituents of a stripping gas stream, regardless of the source of the stripping gas stream, using a membrane disposed within a plenum, said membrane having an upstream side and an opposite downstream side, said stream including stripping gases, water vapor, and stripped product gas, wherein said stripped product gas includes ammonia and/or volatile biomass fermentation products including butanol and other alcohols, comprising the steps of:
(a) conveying the stripping gas stream to the upstream side of the membrane, said membrane having a high permeability rate for water and a lower permeability rate for the stripping gas;
(b) applying a differential pressure between the upstream side of the membrane and the downstream side of the membrane, whereby water vapor passes through the membrane to the downstream side of the membrane as water vapor permeate, and the gas on the upstream side of the membrane becomes depleted of water vapor as retentate gas;
(c) condensing the retentate gas formed in step (b) in a condenser to form condensate product and retentate gas that is deficient in said condensate product; and
(d) combining the water vapor permeate formed in step (b) with the retentate gas that is deficient in condensate product to form a combined stripping gas.
2. The process of claim 1, wherein the microorganisms include heterotrophic microorganisms capable of converting the substrate into alcohols whereby the stripped gas includes butanol or other linear or branched chain alcohols.
3. The process of claim 2, wherein the microorganisms include Clostridium acetobutylicum.
4. The process according to claim 2, further comprising inserting the stripped gas into a condenser cooled by a chiller and operating at a temperature less than the temperature of the liquid in the vessel, whereby the stripped gas and water vapor are condensed to form a condensate product and a gas that is deficient in said product.
5. The process of claim 4, further comprising recirculating the gas that is deficient in said product past the growth plates for further stripping.
6. The process of claim 5, wherein if the temperature of the gas that is deficient in said product is less than the temperature of the liquid in the vessel, further comprising heating said gas up to said temperature and recirculating said heated gas past the growth plates for further stripping.
7. The process of claim 5, further comprising discharging excess stripping gas and/or providing make up stripping gas through a pressure and vacuum relief valve.
8. The process according to claim 5, wherein the stripping gas includes one or more of air, methane, nitrogen and/or oxygen, comprising further concentrating the product by the steps of:
(a) conveying the stripped gas to an upstream side of a membrane disposed within a plenum, said membrane having a high permeability rate for water and a lower permeability rate for the stripping gas, and said stripping gas stream comprising stripping gas, water vapor, and stripped gas;
(b) applying a differential pressure between the upstream side of the membrane and an opposite downstream side of the membrane, whereby water vapor passes through the membrane to the downstream side of the membrane as water vapor permeate, and the gas on the upstream side of the membrane becomes depleted of water vapor as retentate gas; and
(c) combining the water vapor permeate formed in step (b) with the retentate gas that is deficient in condensate product to form a combined stripping gas.
9. The method of claim 1, wherein a gas is introduced into the rotating bioreactor contactor above the influent stream to increase the growth rate of said microorganisms.
10. The method of claim 9, wherein the rotating bioreactor contact has been converted into a rotating photobioreactor by equipping the rotating bioreactor contactor with a light source directed at the microorganisms, said microorganisms include autotrophic microorganisms, and said introduced gas comprises carbon dioxide.
11. The method of claim 9, wherein said microorganisms include heterotrophic microorganisms and said introduced gas comprises oxygen.
13. The process of claim 12, further comprising passing the combined stripping gas past the growth plates of a rotating photobioreactor, said rotating photobioreactor including a vessel, a shaft mounted for rotation within said vessel about a shaft axis, a plurality of axially spaced-apart, growth plates attached to the shaft, each of the plates having surfaces to which a fixed film of the microorganisms are attached, means for rotating the shaft and plates about the axis at a user-selectable rotational speed, and illumination means, while simultaneously performing the steps of:
(a) shining light upon the microorganisms with the illumination means;
(b) optionally feeding a carbon source into the vessel; and
(c) feeding the influent stream past the growth plates such that the growth plates are partially submerged within the stream, whereby, as they grow, the microorganisms remove nutrients from the influent stream, capture the nutrients in biomass, emit oxygen gas, and convert the influent stream to a nutrient-deficient effluent stream; and
further comprising
(d) using the harvesting means to remove a portion of the microorganisms from the surfaces of the growth plates.
14. The process of claim 13, further comprising passing the combined stripping gas through a heater to raise the temperature thereof up to the temperature of the liquid in the vessel, and then passing the heated, combined stripping gas past the growth plates.
15. The process according to claim 13, wherein the differential pressure across the membrane is maintained by a recirculating blower and control valve to cause the return flow of water vapor permeate with its latent heat to the rotating photobioreactor.
16. The process according to claim 12 or 13 wherein the condensate product comprises aqua ammonia concentrated to 10 percent (w/w) or more, suitable for use in the pretreatment of lignocellulosic biomass for renewable energy production.
17. The process according to claim 12, 13 or 14, wherein the condensate product comprises a highly concentrated aqua ammonia concentrated to 20 percent (w/w) or more, suitable for use as diesel exhaust fluid.
18. The process of claim 14, wherein the differential pressure across the membrane is maintained by a recirculating blower and control valve to cause the return flow of water vapor permeate with its latent heat to the rotating photobioreactor.

This is a divisional of U.S. patent application Ser. No. 13/987,795 filed on Sep. 3, 2013, now U.S. Pat. No. 8,895,279. This application claims the benefit of provisional Application No. 61/743,380 by the same applicant for the same invention, filed Sep. 4, 2012, and is a continuation-in-part of application Ser. No. 13/373,860, filed on Dec. 1, 2011. application Ser. No. 13/373,860 claims the benefit of provisional Application No. 61/460,219, filed Dec. 29, 2010. All of the above are incorporated herein expressly by reference in their entirety.

The U.S. Department of Agriculture funded proof of concept research under U.S. Department of Agriculture 2010 SBIR project number 2010-33610-20920.

1. Field of Invention

This invention is a bioreactor that can support a large fixed microbial or autotrophic biofilm that consumes soluble organic or inorganic substrates while producing a nutrient rich biomass and gases such as hydrogen, oxygen, biofuels, and ammonia, that are harvested for a beneficial purpose. This invention can be applied to a variety of processes for recovering valuable gases, nutrients, and products produced from different substrates by autotrophic organisms in a single reactor without the use of chemicals and with minimal energy inputs. Applications include nutrient removal and harvesting from a variety of water bodies, volatile or semi-volatile gas stripping, concentration of stripped gases, and compost biogenic drying.

2. Background

Nutrients discharged from agricultural operations, waste management, and bioenergy processing facilities are significant environmental problems adversely affecting over 30% of our nations waters. The National Academy of Engineering of the National Academies recently published the “Grand Challenges for Engineering,” posted at http://www.engineeringchallenges.org/_cms/challenges.aspx. One of the 14 challenges was “Manage the Nitrogen Cycle”. The “nitrogen issue” is the result of twice as much nitrogen being introduced into the world through anthropogenic sources as introduced from natural sources. The ability to produce reactive nitrogen through the Haber-Bosch process has enabled man to feed the world. However, that engineering miracle has totally distorted the nitrogen cycle leading to significant environmental and public health problems. Seventy five percent of the additional anthropogenic reactive nitrogen input is converted to N2 gas through denitrification, a process that converts a portion (2% to 6%) of the nitrogen to the powerful greenhouse gas N2O, which has an atmospheric lifetime of over 100 years. Aside from being a powerful GHG at 310 times CO2, N2O is now the primary cause of stratospheric ozone depletion. The remaining 25% of the added reactive nitrogen is accumulated in the soils, groundwater, rivers, estuaries, and oceans modifying those terrestrial and aquatic environments. The adverse impacts of nitrogen include the production of fine particulate matter that is responsible for atmospheric haze and increased human mortality, increased nitrate levels in groundwater, acidification of surface water, harmful toxin producing algae blooms, hypoxia in coastal waters, forestry decline, and loss of terrestrial biodiversity.

Solutions to the “nitrogen problem” have primarily been through the use of engineered denitrification systems that increase the NOx, N2O, and fine particulate matter emissions to the atmosphere. Some processes attempt to recover and reuse ammonia and thereby reduce the industrial production of ammonia through the Haber-Bosch process. Ion exchange, membrane separation, and stripping technologies have all been used. The recovery processes invariably sequester the ammonia as dilute acidic solutions of ammonium sulfate or ammonium nitrate. Those processes have been shown to be uneconomical technologies.

Soluble phosphorus and nitrogen are the primary concern. Technology is required to economically remove soluble nitrogen, phosphorus, and potassium nutrients discharged from waste treatment, agricultural fields, or bioenergy facilities. Such facilities include manure management, food processing, wastewater treatment, and renewable energy production such as anaerobic digestion where a majority of the particulate organic nutrients are converted to soluble ammonia and phosphate.

A large variety of expensive technologies have been developed to remove both soluble nitrogen and phosphate from wastewater streams. Phosphate removal by chemical precipitation, biological assimilation, or crystallization (MAP, struvite) precipitation is expensive. Ammonia nitrogen removal by stripping, biological nitrification/denitrification, ammonia oxidation (Anammox) or precipitation as ammonium sulfate, nitrate, or phosphate is also expensive. Wetlands or constructed marshes are the least expensive but occupy large tracts of land where nutrient accumulation may not be sustainable.

Conversion of soluble nutrients to particulate matter, such as micro and macro algae is an attractive method for removing soluble nutrients. However, the limited productivity, ammonia toxicity, and cost of harvesting have prevented widespread adoption. Algae or cyanobacteria growth is limited by the turbidity that such growth imparts to the liquid. Light penetration is reduced in direct proportion to the algae biomass concentration. Pond surface area also limits CO2 transfer to the growing algae thereby limiting productivity. Variable depth and energy consuming gas injection photobioreactors have been proposed to overcome such limitations.

Ammonia toxicity is also a significant problem requiring dilutions of up to 20 to 1 for anaerobic digestate. Ammonia concentrations exceeding 100 ppm are inhibitory to autotrophic growth. Nitrogen loss to the atmosphere is also a significant problem in high pH systems. The loss of nitrogen to the atmosphere led the National Academy of Science to conclude that the growth of algae for biofuel production was unsustainable. “The estimated requirement for nitrogen and phosphorus needed to produce algal biofuels necessary to meet 5% of US transportation fuel ranges from 6 million to 15 million metric tons of nitrogen and from 1 million to 2 million metric tons of phosphorus if the nutrients are not recycled or included and used in co-products. Those estimated requirements represent 44 to 107 percent of the total nitrogen use and 20 to 51 percent of total phosphorus use in the United States.”

Finally, harvesting a highly concentrated biomass containing the recovered nutrients is expensive. The algae biomass separation and concentration is the most expensive unit process, representing 20 to 30% of the total cost of algae production and recovery systems. The limited productivity results in slow nutrient recovery in larger than desired reactors. Additional equipment for biomass nutrient separation and concentration increases the cost considerably.

The autotrophic rotating photobioreactor (RPB) is similar to the heterotrophic rotating biological contactor (RBC), a waste treatment device used to support large heterotrophic bacterial populations for the enhanced removal of soluble organic waste constituents flowing through the RBC. In fact, a rotating bioreactor contactor can be converted into a rotating photobioreactor by adding to it a light source directed at the microorgisms, using autotrophic micoorganisms, and providing a carbon source, such as carbon dioxide or bicarbonate. A variety of configurations and devices exist for heterotrophic waste treatment. The following U.S. patents are representative of the development of the art: U.S. Pat. No. 1,811,181 (an original disclosure of an open RBC, issued in 1931); U.S. Pat. No. 1,947,777 (an enclosed heat exchanger, adsorption unit, issued in 1934); U.S. Pat. No. 3,630,366 (the typical open conventional RBC, issued in 1971); U.S. Pat. No. 3,704,783 (an aerated fixed film RBC, issued in 1972); U.S. Pat. No. 3,904,525 (a pre-aerated spray RBC issued in 1975); U.S. Pat. No. 4,115,268 (an open or closed RBC with an alternative rotor design, issued in 1978); U.S. Pat. No. 4,137,172 (an attached growth RBC with corrugated disks, operating at 40% submergence, issued in 1979); U.S. Pat. No. 4,289,620 (a RBC in combination with an adsorbent, issued in 1981); U.S. Pat. No. 4,330,408 (a partially submerged RBC incorporating suffusing a portion of disc with air, issued in 1982); U.S. Pat. No. 4,345,997 (an RBC with unique disc ribs, issued in 1982); U.S. Pat. No. 4,385,987 (a RBC with alternative structural design of the discs, issued in 1983); U.S. Pat. No. 4,431,537 issued in 1984; U.S. Pat. No. 4,444,658 issued in 1984); U.S. Pat. No. 4,537,678 issued in 1985); U.S. Pat. No. 4,549,962 issued in 1985); U.S. Pat. No. 5,401,398 issued in 1995); U.S. Pat. No. 5,458,817, issued in 1995); U.S. Pat. No. 5,498,376 issued in 1996; U.S. Pat. No. 5,637,263 issued in 1997); U.S. Pat. No. 5,714,097 issued in 1998); U.S. Pat. No. 5,851,636 (ceramic plates) issued in 1998); U.S. Pat. No. 6,071,593 (grooved ceramic packing) issued in 2000); U.S. Pat. No. 6,241,222 issued in 2001); U.S. Pat. No. 6,783,669 issued in 2004); U.S. Pat. No. 7,156,986 issued in 2007); U.S. Pat. No. 8,460,548 issued in 2013); U.S. Pat. No. 4,563,282 (a RBC incorporating microscreens in conjunction with rotating biological contactors that are placed in a primary settling tank, the aeration tank and a final clarification tank, issued in 1986); U.S. Pat. No. 4,568,457 (an anaerobic RBC incorporating acid and methane phase segments, issued in 1986); U.S. Pat. No. 4,604,206 (a staged anaerobic digestion RBC, issued in 1986); U.S. Pat. No. 4,668,387 (an aerated, completely submerged air-driven RBC, issued in 1987); U.S. Pat. No. 4,692,250 (a recirculating staged waste water treatment RBC, issued in 1987); U.S. Pat. No. 4,721,570 (a RBC with a solids contact zone, issued in 1988); U.S. Pat. Nos. 4,729,828 and 4,737,278 (a modular rotating biological contactor apparatus, issued in 1988); U.S. Pat. No. 5,326,459 (a two-stage RBC with different diameter discs, issued in 1994); U.S. Pat. No. 5,395,528 (a complex sewage treatment apparatus incorporating a RBC, issued in 1995); U.S. Pat. No. 5,407,578 (a partitioned RBC capable of addressing toxic inputs, issued in 1995); U.S. Pat. No. 5,853,591 (a hydraulically driven RBC, issued in 1998); U.S. Pat. No. 6,403,366 (a rotating biofilter scrubber for removing air pollutants, issued in 2002); U.S. Pat. No. 7,083,720 (a modular expandable RBC, issued in 2006); U.S. Pat. No. 8,191,868 (a Rotating Inverse Biological Contactor (RIBC), issued in 2012); and U.S. Pat. No. 8,398,828 (an RBC incorporating photocatalytic degradation with UV light, issued in 2013). Relevant U.S. patent applications include: No. 20050133444 (self-cleansing media, filed in 2005); a patent application for a double-sided, self-cleaning media, filed in 2007; No. 20080053880 (configurable RBC application, filed in 2008); No. 20080210610 (RBC that could be inoculated with various bacteria, filed in 2008).

The patent history displays a wide variety of configurations and arrangements for the aerobic or anaerobic treatment of wastewater through the retained growth of a bacterial biofilm on the RBC rotating surface in open or enclosed reactors. A large heterotrophic, as opposed to autotrophic biomass population is achieved, but gases are not managed and stripping of end products has not been practiced.

U.S. patent application Ser. No. 13/373,860 of Burke, entitled Ammonia Nitrogen Recovery Through a Biological Process, filed on Dec. 1, 2011, disclosed use of a biofilm in a rotating photobioreactor (RBC) to support bicarbonate consumption through the growth of autotrophic organisms, thereby increasing the pH and shifting ammonium to ammonia gas for subsequent stripping. That application claimed a process whereby the pH was increased and the ammonia gas stripped in the same reactor without the use of chemicals, as shown in FIG. 2. Ammonia gas was produced and stripped, thereby reducing end-product inhibition while maintaining concentrated biomass for maximum ammonium to ammonia conversion. The configuration specified in U.S. patent application Ser. No. 13/373,860 has many other applications, some of which are the subject of the present invention. Important benefits of the process include the support of a large retained biomass population as a fixed film, removal of inhibitory end products while they are produced, ease of harvesting the biomass, and low energy inputs.

The rotating photobioreactor (RPB) was developed to overcome the nutrient removal limitations associated with conventional autotrophic organism growth in ponds or reactors. The rotating photobioreactor (RPB) is an improved method of producing biomass for energy production, as well as removing and concentrating nutrients from waste streams and/or eutrophic waters. The bioreactor is capable of providing high surface to volume ratios (S/V) for maximum light exposure, photo-autotrophic growth, gas transfer, and oxygen production. The RPB can be open or enclosed. It can be mounted in a vessel such as a tank or placed in a water body. “Vessel” is broadly defined to include, without limitation, a container, receptacle, repository such as a tank, water body, lake, river or stream, liquid conveyance or transport channel. The RPB enables efficient harvesting of concentrated nutrient laden biomass. Those attributes make the RPB an attractive, simple, economical, and scalable method for removing soluble nutrients (NPK) from waste streams. The process is a low head gas production and management apparatus that produces oxygen, while consuming CO2. The RPB is a sustainable nutrient waste treatment technology that incorporates a method to economically concentrate and separate the nutrient laden, biomass for use as a fertilizer or renewable energy source.

The RPB was originally developed as a method to increase the pH of anaerobic digestate without the use of chemicals for the stripping and recovery of ammonia nitrogen (Burke, U.S. patent application Ser. No. 13/373,860, entitled Ammonia Nitrogen Recovery Through a Biological Process, filed Dec. 1, 2011). It was known that autotrophs consume bicarbonate and thereby increase the liquid pH when the amount of carbon dioxide present is low enough to be growth limiting. However, the use of algae or cyanobacteria presented a number of problems. Ammonia is toxic to autotrophs and significantly reduces their specific growth rate. Consequently, it was necessary to develop a large biomass for sufficient growth to occur and thereby consume the bicarbonate to provide an increased pH at low specific growth rates. The development of a large cyanobacterial mass required a large phototrophic surface to volume ratio (S/V). But developing a large surface to volume ratio was hindered by the color and turbidity of the digestate as well as turbidity produced through autotrophic growth. The color, turbidity, and autotrophic concentration reduced the photic zone in which autotroph growth occurs. All of those deficiencies can be overcome by using attached autotrophic growth apparatus, i.e., the RPB. Growth occurs on plates or rotating solid or semisolid surfaces constructed of a variety of materials upon which organisms attach and form a biofilm.

The process/apparatus, called an attached growth, rotating photobioreactor (RPB), uses natural or genetically-engineered organisms that attach to a rotating support media upon which autotrophic organisms grow. The media consists of a series of plates or plate-shaped media that maximize light exposure and gas exchange within an enclosed or open reactor. An example of the apparatus is as shown in FIG. 1. The attributes of the process are as follows:

In contrast, the RPB attached biomass can be easily harvested. The concentrated solids can be removed from the rotating plates through any of a variety of means such as periodic scraping or partial scraping with a blade to discharge the aggregated solids to the liquid media for removal through settling. Concentrated biomass is preferably removed from the rotating surface of the growth plates with a vacuum suction device that periodically removes a portion of the biomass from different sections of the rotating surface like a record player stylus. Concentrated biomass at 10% plus is accumulated in a vacuum receiver. That biomass can be delivered to an energy producing process to recover the energy value as an oil, sugar, or biomethane gas. The biomass may also be further dried to produce a fertilizer in a powder or pellet form.

“Volatile” is broadly defined to include, without limitation, an evaporative or vaporous substance such as water, alcohol, and gases such as ammonia (NH3) that are evaporated at normal temperatures. Unlike conventional photobioreactors, the gas supply containing CO2 is delivered at low atmospheric pressure. In other processes, such as butanol production, the toxic end product, butanol can be easily removed by blowing gas across the surface of the plates as shown in FIG. 2, as opposed to energy-consuming gas stripping through foam-producing bubble aeration.

Foam is not produced with such an arrangement. The disclosed process of stripping in attached growth bioreactors can be applied to heterotrophic (FIG. 3-B) as well as autotrophic (FIG. 3-A) reactors.

FIG. 1-A presents a general plan of a covered or uncovered rotating photobioreactor; and

FIG. 1-B is an elevational view thereof.

FIG. 2 is an elevational view of volatile gas stripping and recovery utilizing the rotating photobioreactor as a combined bioreactor and stripping unit.

FIG. 3-A presents volatile gas stripping and concentration utilizing the rotating photobioreactor as a combined bioreactor, stripping, concentration and recovery unit.

FIG. 3-B presents volatile gas stripping and concentration utilizing the rotating biological contactor as a combined bioreactor, stripping, concentration and recovery unit.

FIG. 4 presents the rotating photobioreactor integrated with a composting/drying reactor process.

FIG. 5-A presents an example of the membrane water vapor separation system; and

FIG. 5-B presents a cross-sectional view thereof.

The rotating photobioreactor (RPB) is a fixed film reactor upon which autotrophic organisms are grown as a biofilm. A basic schematic of the reactor is shown in FIGS. 1-A and 1-B. It consists of a series of solid or semi-solid rotating plates or discs (5) that support the growth of a biofilm. The photobioreactor can be open or closed, covered (10) or uncovered. It can be mounted in a vessel such as a reactor tank (9), stream channel or water body, waste conveyance channel, etc. The reactor can use natural or artificial light (6). Lighting can be above (6), between (11), or below the rotating discs. The discs are supported on a shaft (8) and driven by any of a variety of drives (7) that can impart a rotating movement to the media.

The media upon which the autotrophic organisms are grown may consist of a variety of substances such as wood, cloth, porous ceramics, glass fiber, carbon fiber, etc. Modifying the topography or roughness of the surface can increase the plate area. The RPB may incorporate a variety of biomass harvesting devices (20) such as doctor blades that remove excess biomass growth and discharge the mass to the liquid stream for downstream removal. Vacuum suction devices may remove excess growth from any portion of the rotating discs and discharge the concentrated solids to a vacuum receiver.

Operation of the rotating photobioreactor requires an influent stream (1) containing essential nutrients, light (6), and a carbon source such as air with carbon dioxide (3), carbon dioxide, or bicarbonate. While recovering nutrients, the reactors produce an effluent gas (4) containing oxygen. The reactor may operate at thermophilic, mesophilic, or psychrophilic temperatures depending on the requirements for the growth of organisms retained on the rotating media.

Growth of the autotrophic organisms removes a portion of the soluble essential nutrients from the influent stream and carbon dioxide from the gas stream to produce particulate biomass that can be harvested (25), thereby removing the essential nutrients from the liquid stream and producing an effluent (2) deficient in nutrients. The rotating photobioreactor may also be used to harvest a variety of gaseous chemicals, such as ammonia, directly or indirectly produced by the autotrophic organisms. The RPB is a unique reactor in that the organisms are exposed to a liquid stream for a portion of the time and a gaseous stream for the remainder of the time. The fraction of the time exposed to either the liquid or the gaseous medium is controlled by the disk submergence or liquid level within the reactor. Products within the influent, or produced in the liquid medium, are carried to the gaseous portion of the reactor and thereby stripped with a circulating gas stream (3).

FIG. 2 presents an illustration of the stripping and recovery process. An influent stream (1) such as anaerobic digestate containing dissolved bicarbonate and dissolved ammonium enters an enclosed (10) rotating photobioreactor (9) having any of a variety of light sources (6) at a lower pH. As a liquid flows through the RPB the autotrophic organisms consume the bicarbonate causing the pH to increase from the influent value to values necessary to causes the ammonium to shift to ammonia gas that can be stripped by a gas flowing over the surface of the rotating plates. Supplemental bicarbonate (HCO3) or carbon dioxide may be added to the influent streams to control growth.

The liquid influent may enter at any of a variety of ports along the lower portion of the reactor. The influent may also contain recirculated effluent to dilute the influent concentration and bicarbonate as required to maintain autotroph growth. The stripping gas (3), deficient in the product to be stripped, enters the upper portion, or gaseous portion, of the RPB at any of a variety of ports along the RPB necessary to achieve optimum gas flow over each plate surface. The stripping gas may exit (4) the RPB at any of a variety of outlet ports along the RPB necessary to achieve optimum product stripping and gas conveyance over each plate surface.

The stripping gas (4) containing the stripped product is conveyed to a condenser (15) cooled by a chiller (12) operating at a temperature less than the photobioreactor wherein the stripped water vapor and product (4) are condensed to form a condensate product (21) to be used for any beneficial purpose. The condenser produces an influent gas (3) deficient in the product that is then conveyed by a blower through a heater, if necessary, to the RPB to provide further stripping. Depending on the application the blower may provide sufficient heat. Excess stripping gas can be discharged and make up gas provided by a pressure and vacuum relief valve (P&VR) (17).

The process of stripping any gas from a liquid stream also removes water vapor that, when condensed, reduces the concentration of the product in the liquid stream since both liquid water and product are produced in the condenser. The concentration of the condensate is directly proportional to the product/water ratio of the stripped gas. As a result most stripping processes produce dilute solutions that have reduced value. In addition to producing a dilute solution the water vapor removes substantial quantities of heat from the reactor. This is a problem inherent in most stripping reactors. Minimizing the gas flow rate, stripping temperature, and condensing at higher temperatures will minimize dilution of the condensate product. Further concentration can be achieved through the use of a gas permeable membrane or membranes (16). The concentration process consists of utilizing a high water vapor permeable membrane such as a silicon gas permeable membrane SSP-M823, available from Specialty Silicone Products, Inc., Ballston Spa, New York, which has a high permeability rate for water vapor (3,500+) and lower permeability rates for ammonia (500), and stripping gases such as methane (80), nitrogen (25), and oxygen (50). The membrane is placed between the stripped gas stream and a plenum. A differential pressure is applied between the stripping gas stream consisting of the stripping gas, water vapor, and ammonia gas (retentate) and the lower pressure plenum gas stream (18)(permeate) composed of water vapor with lower concentrations of the stripping gas and ammonia. After passing through the membrane the stripping gas is depleted of water vapor while the plenum gas (18) is enriched. The plenum gas is then combined with the influent stripping gas from the condensate unit, thereby enriching the stripping gas with heat, water vapor, and minor concentrations of the product such as ammonia without significant loss of latent heat as shown in FIGS. 3-A and 3-B.

As shown in FIGS. 3-A and 3-B, one or more water vapor permeable membranes are installed on the stripping gas stream leaving the reactor, but prior to the chiller/condenser (15). The water permeable membranes are placed under a vacuum by the recirculating blower (11) and control valve (14), or another pressurization device, to cause the return flow of water vapor permeate with its latent heat to the photobioreactor.

The above-described product concentration process can be applied to a variety of stripping processes using a variety of substrates. “Substrate” is broadly defined to include, without limitation, a liquid stream or waste substance containing Nitrogen, Phosphorus, Potassium and other essential nutrients, including light required for autotrophic or heterotrophic organism growth, including organic compounds derived from the pretreatment or hydrolysis of cellulosic or lignocellulosic biomass selected from the group consisting of waste materials corn cobs, crop residues, corn husks, corn stover, grasses, wheat straw, barley straw, hay, rice straw, switchgrass, waste paper, sugar cane bagasse, sorghum, soy, components obtained from milling of grains, trees, branches, roots, leaves, wood chips, sawdust, shrubs and bushes, vegetables, fruits, flowers, animal manure, human waste, sugar, algae, cyanobacteria and mixtures thereof. A highly concentrated aqua ammonia stream has significantly greater value if used in ammonia-soaking pretreatment of lignocellulosic biomass for renewable energy production (12+%) as well as in the production of diesel exhaust fluids (20+%). The membrane system presented here can produce both products.

The product recovery process (FIG. 2) and the product concentration process (FIG. 3-B) described above may also be applied to heterotrophic bioreactors such as the RBC to strip and recover “end products” such as butanol and other alcohols from fermentation processes without producing foam or utilizing excess energy. The RPB may also be integrated with composting or compost drying without producing odors inherent in those processes. Such a low pressure integration is shown in FIG. 4. The photobioreactor (9) is coupled with a solids compost or compost drying reactor (22). The photobioreactor receives a liquid or solid stream containing sufficient nutrients for autotrophic growth and produces a liquid stream deficient in nutrients. The photobioreactor also produces a biomass stream that can be harvested (25) for production of an organic fertilizer, input to the compost dryer, or converted to energy through any of a variety of thermochemical or biological processes such as anaerobic digestion. The photobioreactor also produces oxygen that can be stripped and transported through a suction or discharge blower (11) with or without a gas heat exchanger (27) to the enclosed biogenic compost dryer (22). Wet solids (20) are also input into the compost dryer with or without photobioreactor harvested biomass. The highly oxygenated organic biomass reacts in the reactor (22) producing carbon dioxide, heat, and water vapor. The reduced and biogenically dried organic compost is discharged from the reactor (22). The carbon dioxide enriched circulating gas stream containing heat and water vapor exits the compost reactor. The carbon dioxide gas stream may be cooled (26) and the condensate (24) recovered, a portion of which may be used in the photobioreactor. Cooling for condensate recovery (26) and heating (27) for the compost/dryer may be provided by a heat pump (23). The CO2 produced in the compost/dryer (22) is then used in the photobioreactor to produce biomass and oxygen in the photobioreactor in a closed loop system. The process provides a means of compost drying without discharging odorous gases to the environment.

Burke, Dennis A.

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